Ziprasidone formulations
Ziprasidone formulations, including controlled-release formulations, formulations containing ziprasidone dihydrochloride, and combinations of ziprasidone and an additional active agent are described.
1 . A formulation, comprising:
an active agent, wherein the active agent is ziprasidone or a pharmaceutically acceptable salt thereof, wherein the active agent has a mean particle size greater than 85 micrometers; and
a pharmaceutically acceptable carrier.
2 . The formulation of claim 1 , wherein the active agent mean particle size is about 88 to about 150 micrometers.
3 . (canceled)
4 . The formulation of claim 1 , wherein the active agent median particle size is less than about 50 micrometers.
5 . (canceled)
6 . The formulation of claim 1 , wherein greater than about 25 percent of the active agent particles above the median particle size have a particle size about 5 to about 50 micrometers.
7 . The formulation of claim 1 , wherein greater than about 50 percent of the active agent particles above the median particle size have a particle size about 5 to about 50 micrometers.
8 . The formulation of claim 1 , wherein greater than about 75 percent of the active agent particles above the median particle size have a particle size about 5 to about 50 micrometers.
9 . The formulation of claim 1 , wherein the active agent is ziprasidone hydrochloride or ziprasidone monohydrochloride monohydrate.
10 - 11 . (canceled)
12 . The formulation of claim 1 , wherein the formulation provides bioequivalence according to FDA guidelines or criteria.
13 . The formulation of claim 1 , wherein the formulation provides a mean maximum plasma concentration of ziprasidone of about 85 ng/ml in the fed mode.
14 . The formulation of claim 1 , wherein the formulation provides a mean time to maximum plasma concentration of ziprasidone of about 4.5 hours in the fed mode.
15 . The formulation of claim 1 or 9 , wherein the formulation provides a dissolution profile such that at least 70% of the ziprasidone therein dissolves within 45 minutes using a USP-2 apparatus containing 900 ml of aqueous NaH 2 PO 4 buffer, pH 7.5, containing 2% (w/v) sodium dodecyl sulfate, and equipped with paddles stirring at 75 rpm.
16 . A controlled-release dosage form, comprising:
a pharmaceutically effective amount of ziprasidone or a pharmaceutically acceptable salt thereof; and
pharmaceutically acceptable excipients,
wherein the dosage form exhibits a dissolution profile such that at 16 hours after combining the dosage form with a dissolution medium less that about 90 percent of the ziprasidone of ziprasidone salt is released in 500 ml of a dissolution medium at 37° C. in Apparatus 2 (USP, <711> Dissolution, paddle, 50 rpm).
17 . The controlled-release dosage form of claim 16 , wherein the dosage form comprises:
a pharmaceutically effective amount of ziprasidone or a pharmaceutically acceptable salt thereof, and
pharmaceutically acceptable excipients,
wherein the form exhibits a dissolution profile such that
at 1 hour after combining the dosage form with the dissolution medium about 5 to about 15 percent of the ziprasidone or ziprasidone salt is released,
at 2 hour after combining the dosage form with the dissolution medium about 10 to about 25 percent of the ziprasidone or ziprasidone salt is released,
at 4 hour after combining the dosage form with the dissolution medium about 15 to about 35 percent of the ziprasidone or ziprasidone salt is released,
at 8 hour after combining the dosage form with the dissolution medium about 25 to about 50 percent of the ziprasidone or ziprasidone salt is released in 500 ml of dissolution medium at 37° C. Apparatus 2 (USP, <771> Dissolution, paddle, 50 rpm).
18 - 21 . (canceled)
22 . The controlled-release dosage form of claim 16 , wherein the dosage form comprises:
ziprasidone or a pharmaceutically acceptable salt thereof, wherein the form provides a maximum ziprasidone plasma concentration (C max ) and an ziprasidone plasma concentration at about 24 hours after administration (C 24 ), wherein the ration of C max to C 24 is less than about 4:1.
23 . The dosage form of claim 22 , comprising ziprasidone hydrochloride or ziprasidone monohydrochloride monohydrate.
24 - 25 . (canceled)
26 . The controlled-release dosage form of claim 16 , wherein the dosage form comprises:
ziprasidone or a pharmaceutically acceptable salt thereof,
wherein at steady-state the form provides a maximum ziprasidone plasma concentration (C max ), a ziprasidone plasma concentration at about 12 hours after administration (C 12 ), and an ziprasidone plasma concentration at about 24 hours after administration (C 24 ), wherein the average ziprasidone plasma concentration between C max and C 12 is substantially equal to the average ziprasidone plasma concentration between C 12 and C 24 .
27 . (canceled)
28 . The oral dosage form of claim 22 , which provides a C max at between about 5.5 and about 12 hours after administration.
29 - 55 . (canceled)
56 . A dosage formulation, comprising:
ziprasidone or a pharmaceutically acceptable salt thereof; and
a histamine-2 antagonist, wherein the histamine-2 antagonist ranitidine or ranitidine in combination with an additional histamine-2 antagonist.
57 . The formulation of claim 56 , comprising ziprasidone hydrochloride or ziprasidone monohydrochloride monohydrate.
58 . The formulation of claim 56 , wherein the additional histamine-2 antagonist is cimetidine, famotidine, nizatidine or a combination comprising at least one of the foregoing additional histamine-2 antagonists.
59 - 62 . (canceled)